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9/6/12

Food and Drug Administration Drug Recalls - Tampa Personal Injury Blog - keithligorilaw.com

Food and Drug Administration Drug Recalls


Aug 29 Posted by Keith Ligori Law in Did You Know? The Food and Drug Administration routinely recalls drugs that are considered unsafe in the community for whatever reason. Recalls are taken by a specific firm to remove a drug from the market. Unfortunately, some people may already have this drug in their home, which is why it's very important to stay on top of what drugs have been recalled. Usually if the recall is on a larger scale the media will publicize the information. In July 2011, the FDA started a pilot program to notify people of drug recalls even before they are classified. Each Wednesday, the unclassified recalls will be published in the Enforcement Report, and will be listed under the heading, "Recalls Pending Classifications: DRUGS." They will be reposted with their classification once that determination has been made. You can send comments or suggestions to the FDA atCDERRecallPilot@fda.hhs.gov. If you have a medicine that has been recalled, talk to your health care professional about the best course of action. Stores generally have a return and refund policy when a company has announced a recall of its products. Also, if you have experienced any negative side effects from a drug that has or has not yet been recalled, it's important to contact a personal injury attorney as soon as possible. For a list of drugs that our firm handles, please visit our consumer alerts page.

2012 Recalls- From www.fda.gov


August 15, 2012 Hospira Recalls One Lot of Hydromorphone Hydrochloride Injection 2 MG/ML, (C-II) 1 ML Fill In 2.5 ML Carpuject August 14, 2012 Hospira Recalls Three Lots Of Propofol Due To Glass Vial Defect July 25, 2012 DUKAL Corporation recalls selected lots of benzalkonium chloride swabs and antiseptic wipes July 13, 2012 Hospira Recalls Certain Lots of Injectable Carboplatin, Cytarabine, Paclitaxel and Methotrexate July 03, 2012 Bedford Laboratories Recalls Leucovorin Calcium Injection June 28, 2012 Bedford Laboratories Issues Voluntary Hospital/UserLevel Recall Of Vecuronium Bromide For Injection Preservative Free, Lot 2067134, Because Of Health Risk June 05, 2012 Sandoz US Announces Precautionary Recall Of Oral Contraceptive Introvale, Following Report Of Packaging Flaw May 25, 2012 Francks Pharmacy: Compounded Prescription Recall May 12, 2012 Hospira Recalls One Lot Of Hydromorphone Hydrochloride Injection 1 MG/ML, (C-II) 1 ML Fill In 2.5 ML Carpuject, That May Contain More Than The Intended Fill Volume May 02, 2012 Franck's Compounding Lab Recalls Triamcinolone acetonide P.F. 80mg/ml
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9/6/12

Food and Drug Administration Drug Recalls - Tampa Personal Injury Blog - keithligorilaw.com

April 24, 2012 American Regent Recalls Epinephrine Injection, USP, 1:1000, 1mL Ampules Lot #1395 Due to Discoloration and Small Visible Particles April 19, 2012 XROCK INDUSTRIES, LLC Recalls X-ROCK, a Product Marketed as a Dietary Supplement To Support Male Sexual Performance, Due to Unlisted, Potentially Hazardous Ingredient April 17, 2012 Hospira Recalls One Lot of Morphine Sulfate Injection, USP 4 MG/ML, (C-II) 1 ML Fill in 2.5 ML Carpuject, That May Contain More Than The Intended Fill Volume March 31, 2012 Franck's Lab Recalls One Lot of triamcinolone acetonide P.F. 80mg/ml April 02, 2012 American Regent Recalls Cyanocobalamin Injection, USP, 100 mcg/mL, 1ml Vial Lot #s 1662, 1679, 1683 March 09, 2012 Recall of Brilliant Blue G February 16, 2012 Bedford Laboratories Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram per Vial February 24, 2012 Regeneca, Inc. Issues a Voluntary Nationwide Recall of All Lots of Single Capsule RegenErect Because of Potential Health Risks February 24, 2012 Glenmark Generics Inc. Recalls Seven Lots of Norgestimate and Ethinyl Estradiol Tablets USP, 0.18 mg/0.035 mg, 0.215 mg/0.035 mg, 0.25 mg/0.035 mg (Generic) Due to Possibility of Out of Sequence Tablets February 22, 2012 American Regent Initiates Nationwide Voluntary Recall Of Phenylephrine HCl Injection, USP, 1% 5 mL Vial, Lot# 0693 Due To Visible Particles February 17, 2012 McNeil Consumer Healthcare Announces Voluntary Nationwide Recall of Infants TYLENOL Oral Suspension, 1 oz. Grape Due to Dosing System Complaints February 16, 2012 Bedford Laboratories Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram per Vial February 10, 2012 Regeneca, Inc. Issues A Voluntary Nationwide Recall Of A Specific Lot Of RegenArouse Because Of Potential Health Risks February 09, 2012 Wholistic Herbs, Inc. Recalls "Koff & Kold" and "Kold Sore" Because Of Possible Health Risk February 06, 2012 North American Rescue, LLC Announces A Follow-Up to the Recall of Crickit Convenience Kits Related to Nationwide Recall of Triad Povidone Iodine Prep Pads February 02, 2012 Bedford Laboratories Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution, USP, LOT 1877093 January 31, 2012 Pfizer Recalls Lo/Ovral-28 and Norgestrel/Ethinyl Estradiol Tablets Due to Possibility of Inexact Tablet Counts or Out of Sequence Tablets January 27, 2012 One Lot of Aveeno Baby Calming Comfort Lotion Recalled January 27, 2012 Cephalon, Inc. recalls Treanda (bendamustine HCL) for Injection 25mg/Vial Due to Particulate Matter
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9/6/12

Food and Drug Administration Drug Recalls - Tampa Personal Injury Blog - keithligorilaw.com

January 19, 2012 Perfect Image Solutions, LLC Issues Voluntary Recall of Unapproved Product Due to Potential Health Risk January 10, 2012 Bedford Laboratories Issues Guidance On 2011 Voluntary Recall Of Polymyxin B For Injection USP And Vecuronium Bromide For Injection Related To Glass Particles January 08, 2012 Novartis Consumer Health Inc. Recalls Certain Over-The-Counter Products Due to Potential Presence Of Foreign Tablets Or Chipped Or Broken Tablets Or Gelcaps

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